Outlook Therapeutics, Inc.
Approval AI-extracted
LYTENAVA
neovascular age-related macular degeneration
Date
TBD
Approval decision Β· Date TBD estimated
What's at stake A final FDA approval decision on LYTENAVA for neovascular age-related macular degeneration is expected Date TBD.
β€œThe Company expects to resubmit the BLA in June 2026 as a Class 1 resubmission.”

Provenance

1 source on file.

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